You are:
An ambitious Manufacturing Systems (MES) Specialist ready to take on new challenges. As industries head towards Manufacturing and Factory Digitalization, MES stand in the center of manufacturing excellence.
The Work:
- Lead in the design, development, documentation, and implementation of Manufacturing Execution Systems (MES)
- Design/Author/Develop/Configure Electronic Batch Records (EBR)
- Implement MES solutions and integrate with ERP and control equipment
- Documentation of MES configuration and validation of EBRs
- Provide organization oversight for complex systems involving the development of MES
- Work closely with business management and users to strategically define the needs and design solutions that add value
- Partner with business clients and delivery teams to determine appropriate solutions
- Direct the activities of team in the above tasks
- Document and analyze the information needs of the business and ensure appropriate solutions are delivered
- Gather user requirements in relation to controlling and recording manufacturing activities
- Respond to requests for client proposals
- Manage and develop client relationships
- Global System Implementation
- Manage medium-small teams and/or projects
Here's What You Need:
- Minimum of 1 year of experience with PharmaSuite MES solutions in a highly automated Life Sciences manufacturing environment
- Bachelor's Degree or equivalent (minimum 3 years work experience). If Associate's Degree, must have equivalent minimum 6 years work experience
Set Yourself Apart:
- Knowledge of FDA and GMP guidelines
- Understanding of Life Sciences validation processes
- Working knowledge of software Development Life Cycle (SDLC) and support methodologies
- Strong written and oral communication skills
- Ability to work in a team-oriented, collaborative environment
- Ability to facilitate meetings and follow up with resulting action items